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肛门拭子中四种人乳头瘤病毒检测方法的比较。

Comparison of four assays for human papillomavirus detection in the anal canal.

机构信息

The Kirby Institute, Wallace Wurth Building, University of New South Wales, New South Wales, Australia.

The Kirby Institute, Wallace Wurth Building, University of New South Wales, New South Wales, Australia.

出版信息

Clin Microbiol Infect. 2022 Dec;28(12):1652.e1-1652.e6. doi: 10.1016/j.cmi.2022.06.027. Epub 2022 Jul 6.

Abstract

OBJECTIVE

Anal cancer is preceded by high-risk human papillomavirus (HRHPV) infection, predominantly HPV16. No HPV assay is licenced for use in anal screening. We aimed to determine the sensitivity and specificity of four anal canal swab HPV assays to predict high-grade squamous epithelial lesions (HSIL).

METHODS

In a cohort of Australian HIV-positive and negative gay and bisexual men, we compared the sensitivity and specificity of detection of 13 anal HRHPV genotypes by Linear Array (LA), Cobas 4800, EuroArray, and Anyplex II HPV28 (+ and ++ cut offs), compared their ability to predict prevalent anal HSIL, and compared anal canal HRHPV detection with HRHPV isolated from HSIL using laser capture microdissection (LCM).

RESULTS

A total of 475 participants had baseline results available for all four assays (166, 35.0% HIV positive), and 169 participants had a diagnosis of cytological and/or histological HSIL. The HPV16 and any HRHPV detection were highest with Anyplex II HPV28 (+) (156, 32.8% 95% CI 28.6-37.2 and 359, 75.6%, 95% CI 71.5-79.4, respectively). For detection of concurrent HSIL and HPV16, the assay sensitivity was similar, ranging from 49.1%, 95% CI 41.4-56.9 (Anyplex II HPV28 ++) to 55.0%, 95% CI 47.2-62.7 (Anyplex II HPV28 +). For concurrent HSIL and any HRHPV detection, EuroArray was more specific than Anyplex II HPV28 (+) (45.9% 95% CI 40.2-51.7 vs 36.7%, 95% CI 31.3-42.4, p = 0.021) and had comparable specificity with Anyplex II HPV28 (++) (45.9% vs 47.2%, 95% CI 41.5-53.0, p = 0.75). All assays had high sensitivities for predicting HPV16 detected on LCM (92.5-97.5%). Anyplex II HPV28 and EuroArray were significantly more sensitive than LA for lesions caused by non-HPV16 HRHPV types on LCM.

DISCUSSION

Anyplex II HPV28 and EuroArray detected more non-16 HRHPV genotypes than LA. Increasing the Anyplex II HPV28 cutoff improved specificity without compromising sensitivity for detection of concurrent HSIL.

摘要

目的

肛门癌以前是高危型人乳头瘤病毒(HRHPV)感染,主要是 HPV16。目前尚无用于肛门筛查的 HPV 检测方法获得许可。本研究旨在确定四种肛门拭子 HPV 检测方法对预测高级别鳞状上皮内病变(HSIL)的敏感性和特异性。

方法

在澳大利亚 HIV 阳性和阴性的男同性恋和双性恋者队列中,我们比较了线性阵列(LA)、Cobas 4800、EuroArray 和 Anyplex II HPV28(+和++ 截止值)检测 13 种肛门 HRHPV 基因型的敏感性和特异性,比较了它们预测现患肛门 HSIL 的能力,并比较了使用激光捕获显微切割(LCM)检测的 HRHPV 与 HRHPV 分离的 HSIL 之间的 HRHPV 检测。

结果

共有 475 名参与者的四项检测均有基线结果(166 名,35.0% HIV 阳性),169 名参与者被诊断为细胞学和/或组织学 HSIL。Anyplex II HPV28(+)检测 HPV16 和任何 HRHPV 的检出率最高(156 例,32.8%95%CI 28.6-37.2;359 例,75.6%95%CI 71.5-79.4)。对于同时检测 HSIL 和 HPV16,检测的敏感性相似,范围为 49.1%(95%CI 41.4-56.9)(Anyplex II HPV28++)至 55.0%(95%CI 47.2-62.7)(Anyplex II HPV28+)。对于同时检测 HSIL 和任何 HRHPV,EuroArray 的特异性高于 Anyplex II HPV28(+)(45.9%95%CI 40.2-51.7 vs 36.7%95%CI 31.3-42.4,p=0.021),与 Anyplex II HPV28(++)的特异性相当(45.9% vs 47.2%,95%CI 41.5-53.0,p=0.75)。所有检测方法对预测 LCM 检测到的 HPV16 均具有较高的敏感性(92.5-97.5%)。与 LA 相比,Anyplex II HPV28 和 EuroArray 对 LCM 检测到的非 HPV16 HRHPV 型引起的病变具有更高的敏感性。

讨论

Anyplex II HPV28 和 EuroArray 比 LA 检测到更多的非 16 HRHPV 基因型。增加 Anyplex II HPV28 截止值可提高特异性,同时不影响同时检测 HSIL 的敏感性。

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